GB835587A - Improved continuous polymerization process - Google Patents
Improved continuous polymerization processInfo
- Publication number
- GB835587A GB835587A GB3559/57A GB355957A GB835587A GB 835587 A GB835587 A GB 835587A GB 3559/57 A GB3559/57 A GB 3559/57A GB 355957 A GB355957 A GB 355957A GB 835587 A GB835587 A GB 835587A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymerization
- aluminium
- diethyl
- zone
- catalyst
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Abstract
In a continuous polymerization process employing a two-component catalyst the polymerization is carried out in two or more stages in separate vessels and after the first stage only one of the catalyst components is added afresh together with further monomer.ALSO:Olefines are polymerized in a continuous process wherein the olefines and inert liquid diluent are introduced to a first polymerization zone together with a polymerization catalyst obtained by mixing a reducing aluminium compound with a reducible metal compound in an inert liquid diluent, a portion of the resultant polymerization mixture is withdrawn continuously and passed to at least one further polymerization zone to which additional olefines and reducing metal compounds are also continuously introduced and a portion of the resultant polymerization mixture is continuously withdrawn from the further polymerization zone and passed to a separation zone for recovery of the polymer. The polymerization mixture is maintained in both the first and further polymerization zones at 100 DEG to 200 DEG F. and at 1-20 atmospheres, the average residence time in the first zone being 0.5-4 hours and in the further reaction zones, 0.5-2 hours. The olefin is preferably purified from catalyst poisons and may be ethylene, propylene or butylene and these may be copolymerized with one another or with other low molecular weight olefins or diolefines. The reducing aluminium compound is an aluminium hydride or an organo-aluminium compound, e.g. aluminium trimethyl, triethyl, triisopropyl, triphenyl, diethyl bromide, diethyl chloride, diphenyl bromide or diphenyl chloride, ethyl aluminium dihydride, diethyl aluminium hydride or ethoxy aluminium diethyl. The reducible metal compound is of a metal of the A sub-groups of groups 4, 5 or 6 of group 8 of the Periodic Table, e.g. titanium, zirconium, thorium, uranium or chromium and may be a chloride e.g. titanium tetrachloride, bromide, oxychloride, complex fluoride, oxide, hydroxide, alcoholates, acetates, benzoates or acetyl acetonates. The inert liquid diluent is preferably an hydrocarbon or halogenated hydrocarbon such as pentane, hexane, heptane, octane, nonane, decane, benzene, toluene, chlorobenzene or light petroleum. Many details of the catalyst preparation, e.g. temperature and residence time, and of the polymerization, e.g. concentration of the various components, and other conditions are given. The polymer produced may be washed with butyl alcohol or acetone to remove metal contaminant. Polyethylene prepared by this process has a low ash content and may be used as a film-forming material, lubricant additive, or in the formation of moulded or injected plastics.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US567239A US2889314A (en) | 1956-02-23 | 1956-02-23 | Continuous polymerization process and apparatus |
Publications (1)
Publication Number | Publication Date |
---|---|
GB835587A true GB835587A (en) | 1960-05-25 |
Family
ID=24266315
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3559/57A Expired GB835587A (en) | 1956-02-23 | 1957-02-01 | Improved continuous polymerization process |
Country Status (2)
Country | Link |
---|---|
US (1) | US2889314A (en) |
GB (1) | GB835587A (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3188306A (en) * | 1965-06-08 | Processes and apparatus for the handling op polyethylene | ||
LU34129A1 (en) * | 1955-11-05 | |||
US3073810A (en) * | 1956-01-23 | 1963-01-15 | Exxon Research Engineering Co | Method for drying wet solid polymeric material |
BE555478A (en) * | 1956-03-05 | |||
US2983720A (en) * | 1956-04-09 | 1961-05-09 | Exxon Research Engineering Co | Polymerization of butene-1 with catalyst of titanium tetrachloride, aluminum triethyl, and diethyl aluminum chloride |
US2976252A (en) * | 1957-05-10 | 1961-03-21 | Exxon Research Engineering Co | Temperature-staged catalyst pretreatment |
US3004016A (en) * | 1957-06-28 | 1961-10-10 | Phillips Petroleum Co | Polymerization process |
US3067184A (en) * | 1957-12-20 | 1962-12-04 | Phillips Petroleum Co | Production of ethylene-butene copolymer |
US3074922A (en) * | 1958-07-21 | 1963-01-22 | Phillips Petroleum Co | Polymerization process and apparatus |
GB852921A (en) * | 1958-08-07 | 1960-11-02 | Monsanto Chemicals | Improvements relating to polymerisation |
US3136747A (en) * | 1958-08-29 | 1964-06-09 | Union Carbide Corp | Continuous process for polymerizing polyethylene |
US3047558A (en) * | 1959-05-15 | 1962-07-31 | Exxon Research Engineering Co | Pressure staged polymerization process |
US3082195A (en) * | 1959-10-22 | 1963-03-19 | Standard Oil Co | Polymerization process |
BE619910A (en) * | 1960-01-29 | |||
US3035040A (en) * | 1960-02-24 | 1962-05-15 | Phillips Petroleum Co | Reaction process for polymerization |
US3437646A (en) * | 1964-10-21 | 1969-04-08 | Phillips Petroleum Co | Reaction process |
US4016342A (en) * | 1975-03-07 | 1977-04-05 | Exxon Research And Engineering Company | Process and product |
FR2312511A1 (en) * | 1975-05-27 | 1976-12-24 | Naphtachimie Sa | DRY POLYMERIZATION OF OLEFINS IN SERIAL REACTORS |
JPH0725829B2 (en) * | 1986-03-07 | 1995-03-22 | 日本石油株式会社 | Method for producing ethylene polymer |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2373888A (en) * | 1940-05-07 | 1945-04-17 | Phillips Petroleum Co | Apparatus for conducting catalytic reactions |
US2396920A (en) * | 1941-04-10 | 1946-03-19 | Du Pont | Ethylene polymerization process |
US2388178A (en) * | 1942-07-30 | 1945-10-30 | Du Pont | Polymerization process |
US2551145A (en) * | 1943-04-13 | 1951-05-01 | Phillips Petroleum Co | Catalytic cracking system |
US2548003A (en) * | 1945-03-01 | 1951-04-10 | American Viscose Corp | Method and apparatus for handling unstable chemical dispersions |
US2643993A (en) * | 1949-09-13 | 1953-06-30 | Standard Oil Dev Co | Continuous process for copolymerizing styrene and isobutylene |
US2666046A (en) * | 1950-12-22 | 1954-01-12 | Standard Oil Dev Co | Copolymer manufacture |
CH363436A (en) * | 1954-06-08 | 1962-07-31 | Montedison Spa | Product formed as a film, fiber or thread and process for its manufacture |
-
1956
- 1956-02-23 US US567239A patent/US2889314A/en not_active Expired - Lifetime
-
1957
- 1957-02-01 GB GB3559/57A patent/GB835587A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US2889314A (en) | 1959-06-02 |
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